Allele Registry

Canonical Allele Identifier: PA357132

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208861

RCV001035237

RCV002433917

ClinVar Variation:

223174

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gly93Arg	CA357130 NM_000551.4:c.277G>C